Detalhe da pesquisa
1.
Retrospective cohort study of familial hypomagnesaemia with hypercalciuria and nephrocalcinosis due to CLDN16 mutations.
Nephrol Dial Transplant
; 30(4): 636-44, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25477417
2.
Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes.
Nephrol Dial Transplant
; 27(2): 667-73, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21669885
3.
The role of tight junctions in paracellular ion transport in the renal tubule: lessons learned from a rare inherited tubular disorder.
Am J Kidney Dis
; 57(2): 320-30, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-21186073
4.
Impaired paracellular ion transport in the loop of Henle causes familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Ann N Y Acad Sci
; 1258: 177-84, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22731731
5.
Claudin function in the thick ascending limb of Henle's loop.
Ann N Y Acad Sci
; 1165: 152-62, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19538301
6.
Claudin-10 exists in six alternatively spliced isoforms that exhibit distinct localization and function.
J Cell Sci
; 122(Pt 10): 1507-17, 2009 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19383724